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Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites

Reciprocal selective pressures can drive coevolutionary changes in parasites and hosts, and result in parasites that are highly specialized to their hosts. Selection and host co-adaptation are better understood in endoparasites than in ectoparasites, whose life cycles may be more loosely linked to t...

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Autores principales: Talbot, Benoit, Balvín, Ondřej, Vonhof, Maarten J., Broders, Hugh G., Fenton, Brock, Keyghobadi, Nusha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493930/
https://www.ncbi.nlm.nih.gov/pubmed/28680688
http://dx.doi.org/10.1098/rsos.170446
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author Talbot, Benoit
Balvín, Ondřej
Vonhof, Maarten J.
Broders, Hugh G.
Fenton, Brock
Keyghobadi, Nusha
author_facet Talbot, Benoit
Balvín, Ondřej
Vonhof, Maarten J.
Broders, Hugh G.
Fenton, Brock
Keyghobadi, Nusha
author_sort Talbot, Benoit
collection PubMed
description Reciprocal selective pressures can drive coevolutionary changes in parasites and hosts, and result in parasites that are highly specialized to their hosts. Selection and host co-adaptation are better understood in endoparasites than in ectoparasites, whose life cycles may be more loosely linked to that of their hosts. Blood-feeding ectoparasites use salivary proteins to prevent haemostasis in the host, and maximize energy intake. Here we looked for signals of selection in salivary protein genes of ectoparasite species from a single genus (Cimex) that associate with a range of hosts including mammals (bats and humans) and birds (swallows). We analysed two genes that code for salivary proteins that inhibit platelet aggregation and vasoconstriction and may directly affect the efficiency of blood feeding in these species. Significant positive selection was detected at five codons in one gene in all bat-associated species groups. Our results suggest association with bats, versus humans or swallows, has posed a selective pressure on the salivary apyrase gene in species of Cimex.
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spelling pubmed-54939302017-07-05 Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites Talbot, Benoit Balvín, Ondřej Vonhof, Maarten J. Broders, Hugh G. Fenton, Brock Keyghobadi, Nusha R Soc Open Sci Biology (Whole Organism) Reciprocal selective pressures can drive coevolutionary changes in parasites and hosts, and result in parasites that are highly specialized to their hosts. Selection and host co-adaptation are better understood in endoparasites than in ectoparasites, whose life cycles may be more loosely linked to that of their hosts. Blood-feeding ectoparasites use salivary proteins to prevent haemostasis in the host, and maximize energy intake. Here we looked for signals of selection in salivary protein genes of ectoparasite species from a single genus (Cimex) that associate with a range of hosts including mammals (bats and humans) and birds (swallows). We analysed two genes that code for salivary proteins that inhibit platelet aggregation and vasoconstriction and may directly affect the efficiency of blood feeding in these species. Significant positive selection was detected at five codons in one gene in all bat-associated species groups. Our results suggest association with bats, versus humans or swallows, has posed a selective pressure on the salivary apyrase gene in species of Cimex. The Royal Society Publishing 2017-06-21 /pmc/articles/PMC5493930/ /pubmed/28680688 http://dx.doi.org/10.1098/rsos.170446 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Talbot, Benoit
Balvín, Ondřej
Vonhof, Maarten J.
Broders, Hugh G.
Fenton, Brock
Keyghobadi, Nusha
Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
title Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
title_full Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
title_fullStr Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
title_full_unstemmed Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
title_short Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
title_sort host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493930/
https://www.ncbi.nlm.nih.gov/pubmed/28680688
http://dx.doi.org/10.1098/rsos.170446
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